Soumaya Mougou

429 total citations
18 papers, 304 citations indexed

About

Soumaya Mougou is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Soumaya Mougou has authored 18 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Reproductive Medicine. Recurrent topics in Soumaya Mougou's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Soumaya Mougou is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Soumaya Mougou collaborates with scholars based in Tunisia, France and Zambia. Soumaya Mougou's co-authors include Saad Hasan Mohammed Ali, Hatem Elghezal, Meriem Mehdi, Hanène Landolsi, Sonia Brahem, Nouha Bouali, Bruno Francou, Anne Guiochon‐Mantel, Jérôme Bouligand and Lucie Tosca and has published in prestigious journals such as Fertility and Sterility, Archives of Disease in Childhood and Urology.

In The Last Decade

Soumaya Mougou

16 papers receiving 272 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Soumaya Mougou Tunisia 10 121 114 93 87 61 18 304
Shiga Hasuike Japan 6 187 1.5× 107 0.9× 143 1.5× 251 2.9× 57 0.9× 10 393
Tracy M. Clement United States 10 103 0.9× 48 0.4× 86 0.9× 189 2.2× 45 0.7× 14 287
Filippo Zambelli Belgium 13 59 0.5× 187 1.6× 112 1.2× 344 4.0× 92 1.5× 24 561
Pawan Puri United States 10 94 0.8× 104 0.9× 148 1.6× 206 2.4× 21 0.3× 19 351
Miaofei Xu China 10 140 1.2× 49 0.4× 110 1.2× 173 2.0× 18 0.3× 17 318
Maria Beatriz da Fonte Kohek Brazil 11 132 1.1× 123 1.1× 239 2.6× 134 1.5× 30 0.5× 24 421
Melinda J. Murphy United States 11 85 0.7× 133 1.2× 119 1.3× 73 0.8× 23 0.4× 13 331
Maud Giele Netherlands 7 152 1.3× 221 1.9× 201 2.2× 390 4.5× 59 1.0× 7 553
Lluís Bassas Spain 6 117 1.0× 123 1.1× 182 2.0× 238 2.7× 25 0.4× 9 387
TAKAFUMI YAMAZAKI Japan 8 91 0.8× 142 1.2× 278 3.0× 152 1.7× 16 0.3× 12 368

Countries citing papers authored by Soumaya Mougou

Since Specialization
Citations

This map shows the geographic impact of Soumaya Mougou's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Soumaya Mougou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Soumaya Mougou more than expected).

Fields of papers citing papers by Soumaya Mougou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Soumaya Mougou. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Soumaya Mougou. The network helps show where Soumaya Mougou may publish in the future.

Co-authorship network of co-authors of Soumaya Mougou

This figure shows the co-authorship network connecting the top 25 collaborators of Soumaya Mougou. A scholar is included among the top collaborators of Soumaya Mougou based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Soumaya Mougou. Soumaya Mougou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
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Sallem, Amira, et al.. (2023). Factors associated with anxiety and depression in men undergoing fertility investigations: a cross-sectional study. BMC Psychology. 11(1). 299–299. 5 indexed citations
4.
Bouali, Nouha, Bruno Francou, Jérôme Bouligand, et al.. (2017). New MCM8 mutation associated with premature ovarian insufficiency and chromosomal instability in a highly consanguineous Tunisian family. Fertility and Sterility. 108(4). 694–702. 51 indexed citations
5.
Khelil, Amel Haj, et al.. (2017). Y chromosome microdeletions in azoospermic and oligozoospermic Tunisian men. Middle East Fertility Society Journal. 23(4). 268–272. 2 indexed citations
6.
Trabelsi, Saoussen, et al.. (2016). Assessment of MYCN amplification status in Tunisian neuroblastoma: CISH and MLPA combining approach.. PubMed. 93(8-9). 527–31. 2 indexed citations
7.
Bouali, Nouha, Bruno Francou, Jérôme Bouligand, et al.. (2016). NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency. Clinical Genetics. 89(5). 608–613. 21 indexed citations
8.
Bouali, Nouha, Soumaya Mougou, Jérôme Bouligand, et al.. (2015). Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure. Annales d Endocrinologie. 76(6). 671–678. 9 indexed citations
9.
Mougou, Soumaya, et al.. (2015). Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardation. Journal of Pediatric Genetics. 1(1). 63–68. 1 indexed citations
10.
Trabelsi, Saoussen, Soumaya Mougou, Moez Gribaa, et al.. (2014). Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith–Wiedemann syndrome as a sporadic adrenocortical tumor. PubMed. 4. 1–3. 5 indexed citations
11.
Mougou, Soumaya, et al.. (2013). A cytogenetic approach to the effects of low levels of ionizing radiation (IR) on the exposed Tunisian hospital workers. International Journal of Occupational Medicine and Environmental Health. 26(1). 144–54. 33 indexed citations
12.
Mougou, Soumaya, et al.. (2013). Molecular and Phenotypic Characterization of Ring Chromosome 22 in Two Unrelated Patients. Cytogenetic and Genome Research. 140(1). 1–11. 19 indexed citations
13.
Labalme, Audrey, Soumaya Mougou, Moez Gribaa, et al.. (2012). Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia. European Journal of Medical Genetics. 55(8-9). 461–465. 21 indexed citations
14.
Mougou, Soumaya, et al.. (2012). A Combination of Micronucleus Assay and Fluorescence In Situ Hybridization Analysis to Evaluate the Genotoxicity of Formaldehyde. Archives of Environmental Contamination and Toxicology. 64(2). 337–344. 16 indexed citations
15.
Kammoun, Molka, et al.. (2012). 732 Turner Syndrome: A Clinico-Cytogenetic Study of 37 Children. Archives of Disease in Childhood. 97(Suppl 2). A211–A211. 1 indexed citations
16.
Brahem, Sonia, Meriem Mehdi, Hanène Landolsi, et al.. (2011). Semen Parameters and Sperm DNA Fragmentation as Causes of Recurrent Pregnancy Loss. Urology. 78(4). 792–796. 81 indexed citations
17.
Elghezal, Hatem, et al.. (2007). Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4–KCNQ2 genes loci. European Journal of Medical Genetics. 50(6). 441–445. 19 indexed citations
18.
Elghezal, Hatem, et al.. (2004). Large duplication 4q25–q34 with mild clinical effect. Annales de Génétique. 47(4). 419–422. 18 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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2026